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DOI 10.1016/j.bbi.2018.03.018

Медицинская библиотека · Brain, behavior, and immunity · 2018

Adrenal hormones and circulating leukocyte subtypes in stroke patients treated with reperfusion therapy.

Miró-Mur Francesc, Laredo Carlos, Renú Arturo, Rudilosso Salvatore, Zhao Yashu, Amaro Sergio, Llull Laura, Urra Xabier, Planas Anna M, Chamorro Ángel

СтатьяПоддержка исследования: вне правительства СШАПеревод пока не подготовлен

Аннотация

Ischemic stroke sets in motion a dialogue between the central nervous and the immune systems that includes the sympathetic/adrenal system. We investigated the course of immune cells and adrenocortical and adrenomedullary effectors in a cohort of 51 patients with acute stroke receiving reperfusion therapy (intravenous alteplase or mechanical thrombectomy) and its correlation with stroke outcomes and infarct growth. Cortisol increased rapidly and fleetingly after stroke, but 39% of patients who had larger infarctions on admission showed a positive delta cortisol at day 1. It was associated with enhanced infarct growth (p = 0.002) and poor outcome [OR (95% CI) 5.30 (1.30-21.69)], and correlated with less lymphocytes and T cells at follow up. Likewise, fewer circulating lymphocytes, T cells, and Tregs were associated with infarct growth. By contrast, metanephrines did not increase at clinical onset, and decreased over time. Higher levels of NMN correlated with more Treg and B cells. Eventually, complete reperfusion at the end of therapy headed the identification of more circulating Tregs at day 1. Then activation of cortical or medullar compartments of the adrenal gland result in specific signatures on leukocyte subpopulations. Manipulation of the adrenal gland hormone levels warrants further investigation.

Для цитирования: Miró-Mur Francesc, Laredo Carlos, Renú Arturo, Rudilosso Salvatore, Zhao Yashu, Amaro Sergio, Llull Laura, Urra Xabier, Planas Anna M, Chamorro Ángel. Adrenal hormones and circulating leukocyte subtypes in stroke patients treated with reperfusion therapy.. Brain, behavior, and immunity. 2018. DOI: 10.1016/j.bbi.2018.03.018.

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